Arrow International, LLC (A subsidiary of Teleflex, Inc.) - FDA 510(k...
4
Total
4
Cleared
0
Denied
Arrow International, LLC (A subsidiary of Teleflex, Inc.) has 4 FDA 510(k) cleared medical devices. Based in Morrisville, US.
Latest FDA clearance: Mar 2025. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Arrow International, LLC (A subsidiary of Teleflex, Inc.) Filter by specialty or product code using the sidebar.
4 devices
Cleared
Mar 14, 2025
Arrow™ Endurance™ Extended Dwell Peripheral Catheter System (EDC-00818)
General Hospital
113d
Cleared
Dec 20, 2024
Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00620)
General Hospital
140d
Cleared
Aug 30, 2022
Arrow Stiffening Stylet
Cardiovascular
210d
Cleared
Aug 22, 2022
VPS Rhythm DLX Device with TipTracker Technology
General Hospital
195d